| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736847-197737164 | Common:3; Rare:103 | ||||
| chr3:197749595-197749984 | Common:1; Rare:126 | ||||
| chr3:197949893-197950251 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959969-197960245 | Common:1; Rare:96 | ||||
| chr4:337415-337883 | Common:4; Rare:135 | ||||
| chr4:499132-499291 | Common:3; Rare:55 | ||||
| chr4:663625-663719 | Rare:32 | ||||
| chr4:673842-673952 | Rare:47 | ||||
| chr4:674223-674558 | Common:1; Rare:157 | ||||
| chr4:932222-932487 | Common:2; Rare:105 | ||||
| chr4:986912-987163 | Common:3; Rare:85; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113533-1113611 | Common:1; Rare:28 | ||||
| chr4:1289656-1289924 | Common:1; Rare:90 | ||||
| chr4:1309370-1309632 | Common:3; Rare:68 | ||||
| chr4:1720538-1720596 | Rare:11 |